Vaccine and Infectious Disease Organization, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Infect Immun. 2013 Aug;81(8):2861-72. doi: 10.1128/IAI.00339-13. Epub 2013 May 28.
Mycobacterium avium subsp. paratuberculosis is the causative agent of Johne's disease (JD) in cattle. M. avium subsp. paratuberculosis infects the gastrointestinal tract of calves, localizing and persisting primarily in the distal ileum. A high percentage of cattle exposed to M. avium subsp. paratuberculosis do not develop JD, but the mechanisms by which they resist infection are not understood. Here, we merge an established in vivo bovine intestinal segment model for M. avium subsp. paratuberculosis infection with bovine-specific peptide kinome arrays as a first step to understanding how infection influences host kinomic responses at the site of infection. Application of peptide arrays to in vivo tissue samples represents a critical and ambitious step in using this technology to understand host-pathogen interactions. Kinome analysis was performed on intestinal samples from 4 ileal segments subdivided into 10 separate compartments (6 M. avium subsp. paratuberculosis-infected compartments and 4 intra-animal controls) using bovine-specific peptide arrays. Kinome data sets clustered into two groups, suggesting unique binary responses to M. avium subsp. paratuberculosis. Similarly, two M. avium subsp. paratuberculosis-specific immune responses, characterized by different antibody, T cell proliferation, and gamma interferon (IFN-γ) responses, were also observed. Interestingly, the kinomic groupings segregated with the immune response groupings. Pathway and gene ontology analyses revealed that differences in innate immune and interleukin signaling and particular differences in the Wnt/β-catenin pathway distinguished the kinomic groupings. Collectively, kinome analysis of tissue samples offers insight into the complex cellular responses induced by M. avium subsp. paratuberculosis in the ileum and provides a novel method to understand mechanisms that alter the balance between cell-mediated and antibody responses to M. avium subsp. paratuberculosis infection.
分支杆菌副结核亚种是牛结核病(JD)的病原体。分支杆菌副结核亚种感染犊牛的胃肠道,主要定位于并持续存在于回肠远端。虽然有很大比例接触分支杆菌副结核亚种的牛不会发展为 JD,但它们抵抗感染的机制尚不清楚。在这里,我们将一种已建立的牛分支杆菌副结核亚种感染的体内肠道段模型与牛特异性肽激酶组阵列相结合,作为了解感染如何影响感染部位宿主激酶组反应的第一步。将肽阵列应用于体内组织样本代表了使用该技术理解宿主-病原体相互作用的关键和有野心的一步。使用牛特异性肽阵列对 4 个回肠段的 10 个独立隔室进行了肠道样本的激酶组分析(6 个分支杆菌副结核亚种感染隔室和 4 个动物内对照)。激酶组数据集聚类为两组,表明对分支杆菌副结核亚种存在独特的二元反应。同样,也观察到两种分支杆菌副结核亚种特异性免疫反应,其特征是不同的抗体、T 细胞增殖和伽马干扰素(IFN-γ)反应。有趣的是,激酶组分组与免疫反应分组相分离。途径和基因本体分析表明,先天免疫和白细胞介素信号的差异以及 Wnt/β-连环蛋白途径的特定差异区分了激酶组分组。总的来说,组织样本的激酶组分析提供了对分支杆菌副结核亚种在回肠中诱导的复杂细胞反应的深入了解,并提供了一种新的方法来理解改变细胞介导的和针对分支杆菌副结核亚种感染的抗体反应之间平衡的机制。